Back to search

Article

Functional analysis of Ectodysplasin-A mutations in X-linked non-syndromic hypodontia and possible involvement of X-chromosome inactivation

2021-08-13

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Mutations of the Ectodysplasin-A (EDA) gene are generally associated with syndrome hypohidrotic ectodermal dysplasia or non-syndromic tooth agenesis. The influence of EDA mutations on dentinogenesis and odontoblast differentiation have not been reported. The aim of this study was to identify genetic clues for the causes of familial non-syndromic oligodontia and...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
24c20f40-bd90-5194-8bd0-ebe1b8e9bac1
DOI
10.21203/rs.3.rs-602940/v2
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Functional analysis of Ectodysplasin-A mutations in X-linked non-syndromic hypodontia and possible involvement of X-chromosome inactivationDOI 10.21203/rs.3.rs-602940/v2
Select a neighboring publication to make it the new centre.